Polyposis registries

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Polyposis Registries

Polyposis registries (pronunciation: /pɒlɪˈpəʊsɪs 'rɛdʒɪstriːz/) are specialized databases that track and monitor patients with polyposis conditions. The term "polyposis" is derived from the Greek words "polys" meaning "many" and "posis" meaning "small growths".

Polyposis registries are crucial in the field of medical genetics and oncology, as they help in the early detection and prevention of cancer in patients with polyposis syndromes. These registries collect and store comprehensive data about patients, including their medical history, genetic information, and the results of clinical examinations and tests.

Types of Polyposis

There are several types of polyposis conditions that are tracked in these registries. Some of the most common ones include:

  • Peutz-Jeghers syndrome (PJS): This is a genetic condition characterized by the development of polyps in the gastrointestinal tract and pigmented spots on the skin and mucous membranes.
  • Juvenile polyposis syndrome (JPS): This is a rare genetic condition characterized by the development of numerous polyps in the gastrointestinal tract.

Importance of Polyposis Registries

Polyposis registries play a vital role in the management and treatment of polyposis conditions. They allow for:

  • Early detection and prevention of cancer: Regular monitoring of patients in the registry can lead to early detection of polyps and timely intervention, reducing the risk of cancer.
  • Research: The data collected in these registries can be used for research purposes, contributing to the understanding of polyposis conditions and the development of new treatments.
  • Genetic counseling: The genetic information stored in the registries can be used for genetic counseling, helping patients and their families understand the risks and implications of polyposis conditions.

See Also

External links

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